کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5279231 1385621 2009 5 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Selective recognition of Zn2+ by salicylaldimine appended triazole-linked di-derivatives of calix[4]arene by enhanced fluorescence emission in aqueous-organic solutions: role of terminal -CH2OH moietieefs in conjunction with the imine in recognition
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آلی
پیش نمایش صفحه اول مقاله
Selective recognition of Zn2+ by salicylaldimine appended triazole-linked di-derivatives of calix[4]arene by enhanced fluorescence emission in aqueous-organic solutions: role of terminal -CH2OH moietieefs in conjunction with the imine in recognition
چکیده انگلیسی

A series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L2), one -CH2OH (L3) and two -CH2OH (L4)-containing moieties, respectively, in order to bring additional support for ion binding. Based on fluorescence and absorption spectroscopies it has been shown that Zn2+ could be selectively recognized by the Schiff's base core and not by the triazole core among the ten metal ions studied both in methanol and in aqueous solutions of methanol and acetonitrile, wherein the -CH2OH moieties augment the fluorescence response by providing additional coordinations to the Zn2+. Thus L4 exhibited a fluorescence enhancement of ∼65, ∼48 and ∼25-fold in methanol, aqueous solutions of methanol and acetonitrile, with minimum detection limits of 174, 313 and 320 ppb, respectively. Both the excitation and emission wavelengths fall in visible region.

A series of lower rim 1,3-di-derivatives possessing Schiff's base cores were synthesized using triazole unit as linker moiety by further introducing butyl (L2), one -CH2OH (L3) and two -CH2OH (L4)-containing moieties respectively, in order to bring additional support for ion binding. Based on fluorescence and absorption spectroscopies it has been shown that Zn2+ could be selectively recognized by the Schiff's base core and not by the triazole core among the ten metal ions studied both in methanol and in aqueous solutions of methanol and acetonitrile, wherein the -CH2OH moieties augment the fluorescence response by providing additional coordinations to the Zn2+. Thus L4 exhibited a fluorescence enhancement of ∼65, ∼48 and ∼25-fold in methanol, aqueous solutions of methanol and acetonitrile, with minimum detection limits of 174, 313 and 320 ppb, respectively. Both the excitation and emission wavelengths fall in visible region.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Tetrahedron Letters - Volume 50, Issue 23, 10 June 2009, Pages 2730-2734
نویسندگان
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